-
VITEK¿ 2 Gram-negative AST Test Kits (Cards) containing Colistin… recall
FDA
· Biomerieux Inc · Class II
-
Medline Kits: 1) VALVE PACK-LF, Model Number: DYNJ0415366P recall
FDA
· Medline Industries, LP · Class I
-
MAGNETOM Vida Fit recall
FDA
· Siemens Medical Solutions USA, Inc · Class I
-
MAGNETOM Vida (DE) recall
FDA
· Siemens Medical Solutions USA, Inc · Class I
-
MAGNETOM Verio Dot Upgrade recall
FDA
· Siemens Medical Solutions USA, Inc · Class I
-
MAGNETOM Verio Dot recall
FDA
· Siemens Medical Solutions USA, Inc · Class I
-
MAGNETOM Verio recall
FDA
· Siemens Medical Solutions USA, Inc · Class I
-
MAGNETOM Spectra as the following: 1. MAGNETOM Spectra recall
FDA
· Siemens Medical Solutions USA, Inc · Class I
-
MAGNETOM Skyra Fit BioMatrix recall
FDA
· Siemens Medical Solutions USA, Inc · Class I
-
MAGNETOM Skyra fit recall
FDA
· Siemens Medical Solutions USA, Inc · Class I
-
MAGNETOM Skyra (DE) recall
FDA
· Siemens Medical Solutions USA, Inc · Class I
-
MAGNETOM Prisma recall
FDA
· Siemens Medical Solutions USA, Inc · Class I
-
MAGNETOM Lumina (DE) recall
FDA
· Siemens Medical Solutions USA, Inc · Class I
-
MAGNETOM Connectom.X. Model Number: 11371480 recall
FDA
· Siemens Medical Solutions USA, Inc · Class I
-
MAGNETOM Cima.X (DE) recall
FDA
· Siemens Medical Solutions USA, Inc · Class I
-
BIOGRAPH One (DE) recall
FDA
· Siemens Medical Solutions USA, Inc · Class I
-
Biograph mMR. Model Number: 10433372 recall
FDA
· Siemens Medical Solutions USA, Inc · Class I
-
1. EXETER V40 STEM 44MM NO 2, Model recall
FDA
· Howmedica Osteonics Corp. · Class II
-
ZAP-X Radiosurgery System, Model: 300150 recall
FDA
· Zap Surgical Systems · Class II
-
Venclose digiRF Generators, Model VCRFG1, with software 3.35 designed to… recall
FDA
· Bard Peripheral Vascular Inc · Class II
-
JUNCTIONAL EMERGENCY TREATMENT TOOL (JETT) recall
FDA
· North American Rescue LLC. · Class II
-
Atlan Product Name: Atlan A350XL Model recall
FDA
· Draeger, Inc. · Class I
-
Atlan Product Name: Atlan A350 Model recall
FDA
· Draeger, Inc. · Class I
-
Reprocessed ACUSON AcuNav Ultrasound Catheter for intracardiac and… recall
FDA
· Medline Industries, LP · Class I
-
Reprocessed ViewFlex Xtra ICE Catheter to visualize cardiac structures recall
FDA
· Medline Industries, LP · Class I
-
Reprocessed Inquiry Steerable Diagnostics Catheter for electrogram… recall
FDA
· Medline Industries, LP · Class I
-
Reprocessed Webster CS Catheter 10 Electrodes for electrophysiological… recall
FDA
· Medline Industries, LP · Class I
-
Reprocessed Livewire Steerable Electrophysiology Catheter Item Numbers… recall
FDA
· Medline Industries, LP · Class I
-
Sterile Medline Convenience Kits: 1) EXTREMITY PACK… recall
FDA
· Medline Industries, LP · Class I
-
Sterile Medline Convenience Kits: 1) MAJOR PACK L-F… recall
FDA
· Medline Industries, LP · Class I
-
GORE ACUSEAL Vascular Graft recall
FDA
· W L Gore & Associates, Inc. · Class II
-
Artegraft Collagen Vascular Grafts Model Numbers: (1) AG 616, (2) AG 630… recall
FDA
· LeMaitre Vascular, Inc. · Class II
-
Medtronic, Simplera Sensor recall
FDA
· Medtronic MiniMed, Inc. · Class II
-
DxC 500 AU Module w/ISE, DxC 500i, With ISE recall
FDA
· Beckman Coulter, Inc. · Class II
-
Change Healthcare Radiology Solutions software version 14.2.2 recall
FDA
· Change Healthcare Canada Company · Class II
-
AESCULAP ELAN 4 FIXED DURAGUARD LONG. Model Number: GB943R recall
FDA
· Aesculap AG · Class II
-
AESCULAP ELAN 4 FIXED DURAGUARD STANDARD. Model Number: GB942R recall
FDA
· Aesculap AG · Class II
-
NES Reprocessed 2.0mm RX Turbo Elite Laser Atherectomy Catheter recall
FDA
· Northeast Scientific Inc. · Class II
-
NES Reprocessed 1.7mm RX Turbo Elite Laser Atherectomy Catheter recall
FDA
· Northeast Scientific Inc. · Class II
-
NES Reprocessed 1.4mm RX Turbo Elite Laser Atherectomy Catheter recall
FDA
· Northeast Scientific Inc. · Class II
-
NES Reprocessed 0.9mm RX Turbo Elite Laser Atherectomy Catheter recall
FDA
· Northeast Scientific Inc. · Class II
-
NES Reprocessed 2.0mm OTW Turbo Elite Laser Atherectomy Catheter recall
FDA
· Northeast Scientific Inc. · Class II
-
NES Reprocessed 1.7mm OTW Turbo Elite Laser Atherectomy Catheter recall
FDA
· Northeast Scientific Inc. · Class II
-
NES Reprocessed 1.4mm OTW Turbo Elite Laser Atherectomy Catheter recall
FDA
· Northeast Scientific Inc. · Class II
-
NES Reprocessed 0.9mm OTW Turbo Elite Laser Atherectomy Catheter recall
FDA
· Northeast Scientific Inc. · Class II
-
IMPLANT EPIKUT PLUS MT16 3,5X10,0MM recall
FDA
· S.I.N. Implant System Ltda · Class II
-
Getinge 88-Series Washer- Disinfector recall
FDA
· Getinge Disinfection Ab · Class II
-
Cardio Vascular-Allura Centron recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper CV20 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD20/20 OR Table recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD20/20 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD20/15 OR Table recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD20/15 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD20/10 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD20 OR Table recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD20 Biplane OR Table recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD20 Biplane recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD20 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD10 OR Table recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD10/10 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II